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BMC Medical Genetics
|
December 13, 2007
No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease
Pascual Sánchez-Juan, Matthew T Bishop, Alison Green, et al.
Scientific Reports
|
September 8, 2017
High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions
Alessia Franceschini, Simone Baiardi, Andrew G Hughson, et al.
Journal of Neurology
|
November 5, 2022
Sporadic Creutzfeldt-Jakob Disease in the young (50 and below): 10-year review of United Kingdom surveillance
Johnny Tam, John Centola, Hatice Kurudzhu, et al.
Journal of Neurology
|
April 10, 2024
Characterisation of RT-QuIC negative cases from the UK National CJD Research and Surveillance programme
Dominic Ng, Neil Watson, Eugene Ace McDermott, et al.
Age and Ageing
|
May 6, 2024
Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10-year review of United Kingdom surveillance
Eugene Ace McDermott, Neil Watson, Johnny Tam, et al.
Journal of Medical Microbiology
|
February 18, 2022
CPC-containing oral rinses inactivate SARS-CoV-2 variants and are active in the presence of human saliva
Enyia R Anderson, Edward I Patterson, Siobhan Richards, et al.
BMC Research Notes
|
November 18, 2023
Microbial production of the plant flavanone hesperetin from caffeic acid
Erik K R Hanko, João Correia, Caio S Souza, et al.
Journal of Neuropathology and Experimental Neurology
|
June 12, 2018
Sporadic Creutzfeldt-Jakob Disease in a Woman Married Into a Gerstmann-Sträussler-Scheinker Family: An Investigation of Prions Transmission via Microchimerism
Aušrine Areškeviciute, Linea Cecilie Melchior, Helle Broholm, et al.
Molecular Neurobiology
|
July 13, 2023
Conservation of vCJD Strain Properties After Extraction and In Vitro Propagation of PrP<sup>Sc</sup> from Archived Formalin-Fixed Brain and Appendix Tissues Using Highly Sensitive Protein Misfolding Cyclic Amplification
Suzanne Suleiman, Lynne I McGuire, Angela Chong, et al.
Acta Neuropathologica
|
February 17, 2017
Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels
Francesca Lattanzio, Samir Abu-Rumeileh, Alessia Franceschini, et al.
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Search research articles
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Showing results (41-50 of 70) with videos related to
Sort By:
Page
of 7
BMC Medical Genetics
|
December 13, 2007
No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease
Pascual Sánchez-Juan, Matthew T Bishop, Alison Green, et al.
Scientific Reports
|
September 8, 2017
High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions
Alessia Franceschini, Simone Baiardi, Andrew G Hughson, et al.
Journal of Neurology
|
November 5, 2022
Sporadic Creutzfeldt-Jakob Disease in the young (50 and below): 10-year review of United Kingdom surveillance
Johnny Tam, John Centola, Hatice Kurudzhu, et al.
Journal of Neurology
|
April 10, 2024
Characterisation of RT-QuIC negative cases from the UK National CJD Research and Surveillance programme
Dominic Ng, Neil Watson, Eugene Ace McDermott, et al.
Age and Ageing
|
May 6, 2024
Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10-year review of United Kingdom surveillance
Eugene Ace McDermott, Neil Watson, Johnny Tam, et al.
Journal of Medical Microbiology
|
February 18, 2022
CPC-containing oral rinses inactivate SARS-CoV-2 variants and are active in the presence of human saliva
Enyia R Anderson, Edward I Patterson, Siobhan Richards, et al.
BMC Research Notes
|
November 18, 2023
Microbial production of the plant flavanone hesperetin from caffeic acid
Erik K R Hanko, João Correia, Caio S Souza, et al.
Journal of Neuropathology and Experimental Neurology
|
June 12, 2018
Sporadic Creutzfeldt-Jakob Disease in a Woman Married Into a Gerstmann-Sträussler-Scheinker Family: An Investigation of Prions Transmission via Microchimerism
Aušrine Areškeviciute, Linea Cecilie Melchior, Helle Broholm, et al.
Molecular Neurobiology
|
July 13, 2023
Conservation of vCJD Strain Properties After Extraction and In Vitro Propagation of PrP<sup>Sc</sup> from Archived Formalin-Fixed Brain and Appendix Tissues Using Highly Sensitive Protein Misfolding Cyclic Amplification
Suzanne Suleiman, Lynne I McGuire, Angela Chong, et al.
Acta Neuropathologica
|
February 17, 2017
Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels
Francesca Lattanzio, Samir Abu-Rumeileh, Alessia Franceschini, et al.
Page
of 7